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Modified oligonucleotides for mismatch discrimination

a technology of modified oligonucleotides and mismatching, applied in the field of molecular biology, can solve the problem that the potential discriminatory power of short oligonucleotides cannot be easily realized

Inactive Publication Date: 2006-01-12
ELITECHGRP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Thus, the potential discriminatory power of short oligonucleotides cannot be easily realized except under conditions of low stringency.

Method used

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  • Modified oligonucleotides for mismatch discrimination
  • Modified oligonucleotides for mismatch discrimination
  • Modified oligonucleotides for mismatch discrimination

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0220] This example illustrates the synthesis of 5-(Prop-2-ynyl-4-methylbenzoate)-5′-O-(4,4′-dimethoxytriphenylmethyl)-2′-deoxyuridine 3′-[(2-cyanoethyl) N,N-diisopropylphosphoramidite] (3).

5-(Prop-2-ynyl-4-methylbenzoate)-2′-deoxyuridine (1)

[0221] To a mixture of 5-iodo-2′-deoxyuridine (5.0 g, 14.12 mmol), CuI (270 mg, 1.42 mmol), Pd(PPh3)4 (0.82 g, 0.714 mmol), and triethylamine (2.4 mL) in 30 mL of anhydrous DMF was added prop-2-ynyl 4-methylbenzoate (6.10 g, 35.06 mmol). The mixture was stirred under argon for 4 h. and then evaporated to dryness. The residue was triturated in methanol and the excess prop-2-ynyl 4-methylbenzoate that precipitated was filtered away. The filtrate was evaporated and the residue was purified by silica gel chromatography eluting with 10% methanol in ethyl acetate. The pure product fractions were evaporated to dryness and the residue was precipitated from ethyl aceate—ether: 3.14 g (56%) yield; TLC (10% methanol in ethyl acetate), Rf=0.50; 1H NMR (DM...

example 2

Phase 1 Preparation of (2R,5R)-5-(4-amino-3-iodopyrazolo[3,4-d]pyrimidinyl)-2-(hydroxymethyl)oxolan-3-ol (9)

3-Iodo-], 5-dihydropyrazolo[3,4-d]pyrimidin-4-one (4)

[0224] The synthesis of this compound was previously reported by Taylor et. al (Tetrahedron, 48(37):8089-8100 (1992)) using a N-iodosuccinimide. Our synthesis, employing iodine momochloride as the iodinating agent is described below.

[0225] To a 1.0 L solution of 1.2 M sodium acetate was added 4-hydroxypyrazolo[3,4-d]pyrimidine (25 g, 184 mmol) followed by iodine monochloride (46 g, 284 mmol). The mixture was stirred in a sealed container for 4 h. at 110° C. The completed reaction was cooled to room temperature and treated with a solution of 30 g of sodium metabisulfite in 200 mL of water. The white precipitate that formed was filtered and rinsed with cold water. The solid was then dissolved in 200 mL of 3.2 M potassium hydroxide solution. Hydrazine monohydrate (5 mL) was added and the solution was stirred for 15 min. The ...

example 3

[0235] This example illustrates the preparation of N-{3-[1-((2R,5R)-5 {[bis(4-methoxyphenyl)phenylmethoxy]methyl}-4-{[bis(methylethyl)amino](2-cyanoethoxy)phosphinooxy}oxolan-2-yl)-6-amino-4-oxo(5-hydropyrazolo[3,4-d]pyrimidin-3-yl)]propyl}-2,2,2-trifluoroacetamide (22)

3-Iodo-4-methoxypyrazolo[3,4-d]pyrimidine-6-ylamine(14)

[0236] 4-Methoxy-pyrazolo[3,4-d]pyrimidin-6-ylamine (6.75 g, 40.87 mmol) was suspended in an aqueous solution containing sodium acetate (6.0 g, 44.09 mmol) and iodine monochloride (9.12 g, 56.17 mmol) and stirred at 100° C. in a sealed reaction vessel for 24 h. The resulting mixture was cooled to room temperature and treated with a solution of sodium metabisulfite (3.6 g, 18.94 mmol) in 24 mL of water. The solid that formed was filtered, rinsed with water and dried: 6.93 g (58%) yield; TLC (10% methanol in ethyl acetate), Rf=0.57; 1H NMR (DMSO-d6) δ 13.08 (1H, br s, N-1 proton), 10.58 (1H, s, N-5 proton), 6.60 (2H, br s, 6-amino).

[(2R,5R)-5-(6-Amino-3-Iodo-4-me...

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Abstract

Modified oligonucleotides are provided containing bases selected from unsubstituted and 3-substituted pyrazolo[3,4-d]pyrimidines and 5-substituted pyrimidines, and optionally have attached minor groove binders and reporter groups.

Description

CROSS-REFERENCES TO RELATED APPLICATIONS [0001] This application claims the benefit of Provisional application Ser. No. 60 / 186,046, filed Mar. 1, 2000; and continuation-in-part of 09 / 724,959, filed Nov. 28, 2000; and is a continuation-in-part of U.S. Application No. 09 / 640,953, filed Aug. 16, 2000; which is a continuation of U.S. application Ser. No. 09 / 054,832, filed Apr. 3, 1998; and is a continuation-in-part of U.S. application Ser. No. 09 / 431,485, filed Nov. 1, 1999; which is a continuation of U.S. application Ser. No. 09 / 054,830, filed Apr. 3, 1998, now U.S. Pat. No. 6,127,121; the disclosures of each being incorporated herein by reference.STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT [0002] Not applicable. BACKGROUND OF THE INVENTION [0003] This application is in the field of molecular biology relating to the use of oligonucleotides as probes and primers in liquid, solid and mixed phase assays. The application further relates to t...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07H21/04C07B61/00C07H19/06C07H19/10C07H19/16C07H19/20C07H19/23C07H21/00C12Q1/68
CPCC07B2200/11C07H19/06C07H19/10C07H19/16C07H19/20C07H19/23C07H21/00G06F19/22C07H21/02C12Q1/6832C40B40/00C12Q2525/117G16B30/00
Inventor DEMPCY, ROBERTGALL, ALEXANDERLOKHOV, SERGEYAFONINA, IRINASINGER, MICHAELKUTYAVIN, IGORVERMEULEN, NICOLAAS
Owner ELITECHGRP
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